How many of you are still on LDN and any Newbies on LDN now.?
I'm on for 12 yrs now and don't know how I ever survived the dang disease without it.
I still have MS, but for the last 12 yrs, I feel "it does not have me, by the ****s..

I've mentioned this before, but do you all notice how much your hair and nails
grow, so much faster? I am forever trimming my hair and filing my nails. Also,
I've noticed how much faster a wound heals and how much faster an illness
subsides

LDN may not be a cure for MS or anything else, but it sure does make me
feel better.. It must be the raise in endorphins, huh? Us MSers are
usually low on endorphins and obviously we need them!!

I hope you all are keeping up with your LDN daily, even though you may be
taking one of the newer MS modifying drugs, as well. At the 4.5mg dose, it
will not hurt us and certainly may help in our fight to live better with our illness.

Best wishes for you all.